<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>3(6)</volume><submitter>Seki Y</submitter><funding>AMED</funding><funding>Japan Society for the Promotion of Science</funding><pubmed_abstract>&lt;h4>Background&lt;/h4>The Omicron variant of severe acute respiratory syndrome-coronavirus-2 (SARS-CoV-2) was identified in Japan in November 2021. This variant contains up to 36 mutations in the spike protein, the target of neutralizing antibodies, and can escape vaccine-induced immunity. A booster vaccination campaign began with healthcare workers and high-risk groups. The safety and immunogenicity of the three-dose vaccination against Omicron remain unknown.&lt;h4>Methods&lt;/h4>A total of 272 healthcare workers were initially evaluated for long-term vaccine safety and immunogenicity. We further established a vaccinee panel to evaluate the safety and immunogenicity against variants of concern (VOCs), including the Omicron variants, using a live virus microneutralization assay.&lt;h4>Findings&lt;/h4>Tw</pubmed_abstract><journal>Med (New York, N.Y.)</journal><pagination>406-421.e4</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9040508</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Safety and immunogenicity of the Pfizer/BioNTech SARS-CoV-2 mRNA third booster vaccine dose against the BA.1 and BA.2 Omicron variants.</pubmed_title><pmcid>PMC9040508</pmcid><pubmed_authors>Sasaki K</pubmed_authors><pubmed_authors>Suzuki T</pubmed_authors><pubmed_authors>Fukushi S</pubmed_authors><pubmed_authors>Seki Y</pubmed_authors><pubmed_authors>Mizukami T</pubmed_authors><pubmed_authors>Takahashi Y</pubmed_authors><pubmed_authors>Yato Y</pubmed_authors><pubmed_authors>Moriyama S</pubmed_authors><pubmed_authors>Nojima K</pubmed_authors><pubmed_authors>Numata N</pubmed_authors><pubmed_authors>Kuzuoka T</pubmed_authors><pubmed_authors>Hamaguchi I</pubmed_authors><pubmed_authors>Yoshihara Y</pubmed_authors><pubmed_authors>Wagatsuma A</pubmed_authors><pubmed_authors>Maeda K</pubmed_authors><pubmed_authors>Momose H</pubmed_authors></additional><is_claimable>false</is_claimable><name>Safety and immunogenicity of the Pfizer/BioNTech SARS-CoV-2 mRNA third booster vaccine dose against the BA.1 and BA.2 Omicron variants.</name><description>&lt;h4>Background&lt;/h4>The Omicron variant of severe acute respiratory syndrome-coronavirus-2 (SARS-CoV-2) was identified in Japan in November 2021. This variant contains up to 36 mutations in the spike protein, the target of neutralizing antibodies, and can escape vaccine-induced immunity. A booster vaccination campaign began with healthcare workers and high-risk groups. The safety and immunogenicity of the three-dose vaccination against Omicron remain unknown.&lt;h4>Methods&lt;/h4>A total of 272 healthcare workers were initially evaluated for long-term vaccine safety and immunogenicity. We further established a vaccinee panel to evaluate the safety and immunogenicity against variants of concern (VOCs), including the Omicron variants, using a live virus microneutralization assay.&lt;h4>Findings&lt;/h4>Tw</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Jun</publication><modification>2026-05-09T15:10:55.749Z</modification><creation>2025-02-18T23:35:50.243Z</creation></dates><accession>S-EPMC9040508</accession><cross_references><pubmed>35815933</pubmed><doi>10.1016/j.medj.2022.04.013</doi></cross_references></HashMap>